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【结 构 式】

【分子编号】61166

【品名】methyl (Z)-4-[(2R,6S)-6-(2-hydroxyethyl)-5,6-dihydro-2H-pyran-2-yl]-2-butenoate

【CA登记号】

【 分 子 式 】C12H18O4

【 分 子 量 】226.27252

【元素组成】C 63.7% H 8.02% O 28.28%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(IV)

The butenoic ester intermediate (VIII) has been obtained as follows: The condensation of the known aldehyde (I) with phosphonate (II) by means of KHMDS in THF gives the unsaturated ester (III), which is selectively hydrolyzed at its benzoate group by means of K2CO3 in methanol to yield the ethanol derivative (IV). The oxidation of (IV) by means of DMP affords the acetaldehyde (V), which is condensed with the phosphorane (VI) by means of DBU and LiCl in acetonitrile to provide the methyl ketone (VII) (1). Finally, this compound is methylated by means of Me2Zn and Ni(acac)2 in ethyl ether to give the target butenoic ester intermediate (VIII)

1 Paterson, I.; et al.; Total synthesis of the microtubule-stabilizing agent (-)-laulimalide. Org Lett 2001, 3, 20, 3149.
2 Paterson, I.; et al.; Synthesis of the macrocyclic core of laulimalide. Org Lett 2001, 3, 2, 213.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 61164 2-[(2S,6R)-6-(2-oxoethyl)-3,6-dihydro-2H-pyran-2-yl]ethyl benzoate C16H18O4 详情 详情
(II) 41856 methyl 2-[bis(2,2,2-trifluoroethoxy)phosphoryl]acetate 88738-78-7 C7H9F6O5P 详情 详情
(III) 61165 2-{(2S,6R)-6-[(Z)-4-methoxy-4-oxo-2-butenyl]-3,6-dihydro-2H-pyran-2-yl}ethyl benzoate C19H22O5 详情 详情
(IV) 61166 methyl (Z)-4-[(2R,6S)-6-(2-hydroxyethyl)-5,6-dihydro-2H-pyran-2-yl]-2-butenoate C12H18O4 详情 详情
(V) 59559 Dimethyl acetonylphosphonate; Acetylmethylphosphonic acid dimethyl ester; Dimethyl (2-oxopropyl)phosphonate 4202-14-6 C5H11O4P 详情 详情
(VI) 61167 methyl (Z)-4-[(2R,6S)-6-(2-oxoethyl)-5,6-dihydro-2H-pyran-2-yl]-2-butenoate C12H16O4 详情 详情
(VII) 61168 methyl (Z)-4-{(2R,6S)-6-[(E)-4-oxo-2-pentenyl]-5,6-dihydro-2H-pyran-2-yl}-2-butenoate C15H20O4 详情 详情
(VIII) 61169 methyl (Z)-4-{(2R,6R)-6-[(2R)-2-methyl-4-oxopentyl]-5,6-dihydro-2H-pyran-2-yl}-2-butenoate C16H24O4 详情 详情
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